-
1
-
-
0027433854
-
Structure correction and synthesis of the naturally occurring benzothiazinone BMY 40662
-
Kelly, T. R.; Kim, M. H.; Certis, A. D. M. Structure correction and synthesis of the naturally occurring benzothiazinone BMY 40662. J. Org. Chem. 1993, 58, 5855.
-
(1993)
J. Org. Chem
, vol.58
, pp. 5855
-
-
Kelly, T.R.1
Kim, M.H.2
Certis, A.D.M.3
-
2
-
-
0028928412
-
Thiocyanate as a versatile synthetic unit: Efficient conversion of ArSCN to aryl alkyl sulfides and aryl thioesters
-
(a) Toste, F. D.; Laronde, F.; Still, W. J. Thiocyanate as a versatile synthetic unit: Efficient conversion of ArSCN to aryl alkyl sulfides and aryl thioesters. Tetrahedron Lett. 1995, 36, 2949;
-
(1995)
Tetrahedron Lett
, vol.36
, pp. 2949
-
-
Toste, F.D.1
Laronde, F.2
Still, W.J.3
-
3
-
-
0141588652
-
Thiocyanation of Indole. Some Reactions of 3-Thiocyanoindole
-
(b) Grant, M. S.; Snyder, H. R. Thiocyanation of Indole. Some Reactions of 3-Thiocyanoindole. J. Am. Chem. Soc.1960, 82, 2742.
-
(1960)
J. Am. Chem. Soc
, vol.82
, pp. 2742
-
-
Grant, M.S.1
Snyder, H.R.2
-
4
-
-
33749009772
-
Palladium-catalyzed, copper(I)-mediated coupling of boronic acids and benzylthiocyanate: A cyanide-free cyanation of boronic acids
-
Zhang, Z.; Liebeskind, L. S. Palladium-catalyzed, copper(I)-mediated coupling of boronic acids and benzylthiocyanate: A cyanide-free cyanation of boronic acids. Org. Lett. 2006, 8, 4331.
-
(2006)
Org. Lett
, vol.8
, pp. 4331
-
-
Zhang, Z.1
Liebeskind, L.S.2
-
5
-
-
17744407351
-
Synthesis of 5,6-dihydro-4-hydroxy-2-pyrones as HIV-1 protease inhibitors: The profound effect of polarity on antiviral activity
-
(a) Hagen, S. E.; Vara Prasad, J. V. N.; Boyer, F. E.; Domagala, J. M.; Ellsworth, E. L.; Gajda, C.; Hamilton, H. W.; Markoski, L. J.; Steinbaugh, B. A.; Tait, B. D.; Lunney, E. A.; Tummino, P. J.; Ferguson, D.; Hupe, D.; Nouhan, C.; Gracheck, S. J.; Saunders, J. M.; Vanderroest, S. Synthesis of 5,6-dihydro-4-hydroxy-2-pyrones as HIV-1 protease inhibitors: The profound effect of polarity on antiviral activity. J. Med. Chem. 1997, 40, 3707;
-
(1997)
J. Med. Chem
, vol.40
, pp. 3707
-
-
Hagen, S.E.1
Vara Prasad, J.V.N.2
Boyer, F.E.3
Domagala, J.M.4
Ellsworth, E.L.5
Gajda, C.6
Hamilton, H.W.7
Markoski, L.J.8
Steinbaugh, B.A.9
Tait, B.D.10
Lunney, E.A.11
Tummino, P.J.12
Ferguson, D.13
Hupe, D.14
Nouhan, C.15
Gracheck, S.J.16
Saunders, J.M.17
Vanderroest, S.18
-
6
-
-
9844223910
-
4-Hydroxy-5,6-dihydropyrones, potent non-peptide inhibitors of HIV protease
-
(b) Tait, B. D.; Hagen, S.; Domagala, J.; Ellsworth, E. L.; Gajda, C.; Hamilton, H. W.; Vara Prasad, J. V. N.; Ferguson, D.; Graham, N.; Hupe, D.; Nouhan, C.; Tummino, P. J.; Humblet, C.; Lunney, E. A.; Pavlovsky, A.; Rubin, J.; Gracheck, S. J.; Baldwin, E. T.; Bhat, T. N.; Erickson, J. W.; Gulnik, S. V.; Liu, B. 4-Hydroxy-5,6-dihydropyrones, potent non-peptide inhibitors of HIV protease. J. Med. Chem. 1997, 40, 3781.
-
(1997)
J. Med. Chem
, vol.40
, pp. 3781
-
-
Tait, B.D.1
Hagen, S.2
Domagala, J.3
Ellsworth, E.L.4
Gajda, C.5
Hamilton, H.W.6
Vara Prasad, J.V.N.7
Ferguson, D.8
Graham, N.9
Hupe, D.10
Nouhan, C.11
Tummino, P.J.12
Humblet, C.13
Lunney, E.A.14
Pavlovsky, A.15
Rubin, J.16
Gracheck, S.J.17
Baldwin, E.T.18
Bhat, T.N.19
Erickson, J.W.20
Gulnik, S.V.21
Liu, B.22
more..
-
7
-
-
23044459885
-
Regioselective thiocyanation of aromatic and heteroaromatic compounds using ammonium thiocyanate and oxone
-
(a) Wu, G.; Liu, Q.; Shen, Y.; Wu, W.; Wu, L. Regioselective thiocyanation of aromatic and heteroaromatic compounds using ammonium thiocyanate and oxone. Tetrahedron Lett. 2005, 46, 5831;
-
(2005)
Tetrahedron Lett
, vol.46
, pp. 5831
-
-
Wu, G.1
Liu, Q.2
Shen, Y.3
Wu, W.4
Wu, L.5
-
8
-
-
1642276015
-
Iodine=MeOH: A novel and efficient reagent system for thiocyanation of aromatics and heteroaromatics
-
(b) Yadav, J. S.; Reddy, S. B. V.; Shubashree, S.; Sadashiv, K. Iodine=MeOH: A novel and efficient reagent system for thiocyanation of aromatics and heteroaromatics. Tetrahedron Lett.2004, 45, 2951;
-
(2004)
Tetrahedron Lett
, vol.45
, pp. 2951
-
-
Yadav, J.S.1
Reddy, S.B.V.2
Shubashree, S.3
Sadashiv, K.4
-
9
-
-
17744364542
-
Ferric(III) chloride-promoted electrophilic thiocyanation of aromatic and heteroaromatic compounds
-
(c) Yadav, J. S.; Reddy, B. V. S.; Krishna, A. D.; Reddy, C. S.; Narsaiah, A.V. Ferric(III) chloride-promoted electrophilic thiocyanation of aromatic and heteroaromatic compounds. Synthesis 2005, 961.
-
(2005)
Synthesis
, pp. 961
-
-
Yadav, J.S.1
Reddy, B.V.S.2
Krishna, A.D.3
Reddy, C.S.4
Narsaiah, A.V.5
-
10
-
-
0028909777
-
A versatile procedure for the preparation of aryl thiocyanates using N-thiocyanatosuccinimide (NTS)
-
(a) Toste, F. D.; Stefano, V. D.; Still, I. W. J. A versatile procedure for the preparation of aryl thiocyanates using N-thiocyanatosuccinimide (NTS). Synth. Commun. 1995, 25, 1277;
-
(1995)
Synth. Commun
, vol.25
, pp. 1277
-
-
Toste, F.D.1
Stefano, V.D.2
Still, I.W.J.3
-
11
-
-
0033524666
-
A direct synthesis of aryl thiocyanates using cerium(IV) ammonium nitrate
-
(b) Nair, V.; George, T. G.; Nair, L. G.; Panicker, S. B. A direct synthesis of aryl thiocyanates using cerium(IV) ammonium nitrate. Tetrahedron Lett. 1999, 40, 1195;
-
(1999)
Tetrahedron Lett
, vol.40
, pp. 1195
-
-
Nair, V.1
George, T.G.2
Nair, L.G.3
Panicker, S.B.4
-
12
-
-
0037189251
-
Novel process for generating useful electrophiles from common anions using Selectfluor fluorination Agent
-
(c) Syvret, R. G.; Butt, K. M.; Nguyen, T. P.; Bulleck, V. L.; Rieth, R. D. Novel process for generating useful electrophiles from common anions using Selectfluor fluorination Agent. J. Org.Chem. 2002, 67, 4487;
-
(2002)
J. Org.Chem
, vol.67
, pp. 4487
-
-
Syvret, R.G.1
Butt, K.M.2
Nguyen, T.P.3
Bulleck, V.L.4
Rieth, R.D.5
-
13
-
-
0141768471
-
A clay-mediated eco-friendly thiocyanation of indoles and carbazoles
-
(d) Chakrabarty, M.; Sarkar, S. A clay-mediated eco-friendly thiocyanation of indoles and carbazoles. Tetrahedron Lett. 2003, 44, 8131.
-
(2003)
Tetrahedron Lett
, vol.44
, pp. 8131
-
-
Chakrabarty, M.1
Sarkar, S.2
-
14
-
-
0001548384
-
Novel and direct nucleophilic sulfenylation and thiocyanation of phenol ethers using a hypervalent iodine(III) reagent
-
(a) Kita, Y.; Takada, T.; Mihara, S.; Whelan, B. A.; Tohma, H. Novel and direct nucleophilic sulfenylation and thiocyanation of phenol ethers using a hypervalent iodine(III) reagent. J. Org. Chem. 1995, 60, 7144;
-
(1995)
J. Org. Chem
, vol.60
, pp. 7144
-
-
Kita, Y.1
Takada, T.2
Mihara, S.3
Whelan, B.A.4
Tohma, H.5
-
15
-
-
0031471952
-
An efficient p-thiocyanation of phenols and naphtols using a reagent combination of phenyliodine dichloride and lead(II) thiocyanate
-
(b) Kita, Y.; Takada, Y.; Okuno, T.; Egi, M.; Kiyosei, I.; Kawaguchi, C.; Akai, S. An efficient p-thiocyanation of phenols and naphtols using a reagent combination of phenyliodine dichloride and lead(II) thiocyanate. Chem. Pharm. Bull.1997, 45, 1887;
-
(1997)
Chem. Pharm. Bull
, vol.45
, pp. 1887
-
-
Kita, Y.1
Takada, Y.2
Okuno, T.3
Egi, M.4
Kiyosei, I.5
Kawaguchi, C.6
Akai, S.7
-
16
-
-
18744409788
-
Efficient and mild oxidative nuclear thiocyanation of activated aromatic compounds using ammonium thiocyanate and diacetoxyiodobenzene
-
(c) Karande, N. N.; Tiwari, G. B.; Shirodkar, S. G.; Dhoot, B. M. Efficient and mild oxidative nuclear thiocyanation of activated aromatic compounds using ammonium thiocyanate and diacetoxyiodobenzene. Synth. Commun. 2005, 35, 1197.
-
(2005)
Synth. Commun
, vol.35
, pp. 1197
-
-
Karande, N.N.1
Tiwari, G.B.2
Shirodkar, S.G.3
Dhoot, B.M.4
-
17
-
-
29144508510
-
3) in combination with tetraethylammonium bromide as a catalyst for selective and accelerated sulfoxidation
-
3) in combination with tetraethylammonium bromide as a catalyst for selective and accelerated sulfoxidation. Synth. Commun. 2005, 35, 2805;
-
(2005)
Synth. Commun
, vol.35
, pp. 2805
-
-
Salgaonker, P.D.1
Shukla, V.G.2
Akamanchi, K.G.3
-
18
-
-
24944541510
-
Iodine and iodic acid: An efficient reagent combination for iodination of aryl hydroxy ketones
-
(b) Patil, B. R.; Bhusare, S. R.; Pawar, R. P.; Vibhute, Y. B. Iodine and iodic acid: An efficient reagent combination for iodination of aryl hydroxy ketones. Tetrahedron Lett. 2005, 46, 7179;
-
(2005)
Tetrahedron Lett
, vol.46
, pp. 7179
-
-
Patil, B.R.1
Bhusare, S.R.2
Pawar, R.P.3
Vibhute, Y.B.4
-
19
-
-
0035077908
-
Chemoselective N-nitrosation of secondary amines under mild and heterogeneous conditions
-
(c) Zolfigol, M. A.; Choghamarani, A. G.; Shirini, F.; Keypour, H.; Salehzadeh, S. Chemoselective N-nitrosation of secondary amines under mild and heterogeneous conditions. Synth. Commun.2001, 31, 359.
-
(2001)
Synth. Commun
, vol.31
, pp. 359
-
-
Zolfigol, M.A.1
Choghamarani, A.G.2
Shirini, F.3
Keypour, H.4
Salehzadeh, S.5
-
20
-
-
33846195507
-
o-Iodoxybenzoic acid- and tetraethylammonium bromide-mediated oxidative transformation of primary carboxamides to one-carbon dehomologated nitriles
-
(a) Bhalerao, D. S.; Mahajan, U. S.; Chaudhari, K. H.; Akamanchi, K. G. o-Iodoxybenzoic acid- and tetraethylammonium bromide-mediated oxidative transformation of primary carboxamides to one-carbon dehomologated nitriles. J. Org. Chem. 2007, 73, 662;
-
(2007)
J. Org. Chem
, vol.73
, pp. 662
-
-
Bhalerao, D.S.1
Mahajan, U.S.2
Chaudhari, K.H.3
Akamanchi, K.G.4
-
21
-
-
34447274204
-
Direct conversion of aldehydes to acyl azides using tertbutyl hypochlorite
-
(b) Arote, N. D.; Bhalerao, D. S.; Akamanchi, K. G. Direct conversion of aldehydes to acyl azides using tertbutyl hypochlorite. Tetrahedron Lett. 2007, 48, 5661;
-
(2007)
Tetrahedron Lett
, vol.48
, pp. 5661
-
-
Arote, N.D.1
Bhalerao, D.S.2
Akamanchi, K.G.3
-
22
-
-
0036456483
-
A novel and one step procedure for preparation of α-bromo-a,β-unsaturated carbonyl compounds
-
(c) Ramnarayanan, G. V.; Shukla, V. G.; Akamanchi, K. G. A novel and one step procedure for preparation of α-bromo-a,β-unsaturated carbonyl compounds. Synlett2002, 12, 2059;
-
(2002)
Synlett
, vol.12
, pp. 2059
-
-
Ramnarayanan, G.V.1
Shukla, V.G.2
Akamanchi, K.G.3
-
23
-
-
0037532988
-
A mild, chemoselective oxidation of sulfides to sulfoxides using o-iodoxybenzoic acid and tetraethylammonium bromide as catalyst
-
(d) Shukla, V. G.; Salgaonker, P. D.; Akamanchi, K. G. A mild, chemoselective oxidation of sulfides to sulfoxides using o-iodoxybenzoic acid and tetraethylammonium bromide as catalyst. J. Org. Chem.2003, 68, 5422;
-
(2003)
J. Org. Chem
, vol.68
, pp. 5422
-
-
Shukla, V.G.1
Salgaonker, P.D.2
Akamanchi, K.G.3
-
24
-
-
0032936089
-
A mild, chemoselective, oxidative method for deoximation using Dess-Martin periodinane
-
(e) Chaudhari, S. S.; Akamanchi, K. G. A mild, chemoselective, oxidative method for deoximation using Dess-Martin periodinane. Synthesis 1999, 760;
-
(1999)
Synthesis
, pp. 760
-
-
Chaudhari, S.S.1
Akamanchi, K.G.2
-
25
-
-
0032516353
-
Deoximation using Dess-Martin periodinane: Regeneration of ketones from ketoximes
-
(f) Chaudhari, S. S.; Akamanchi, K. G. Deoximation using Dess-Martin periodinane: Regeneration of ketones from ketoximes. Tetrahedron Lett. 1998, 39, 3209.
-
(1998)
Tetrahedron Lett
, vol.39
, pp. 3209
-
-
Chaudhari, S.S.1
Akamanchi, K.G.2
-
27
-
-
0346607454
-
2,2-Diphenyl-3,3- dimethylethylenimine and related compounds
-
(b) Kissman, H. M.; Tarbell, D. S.; Williams. 2,2-Diphenyl-3,3- dimethylethylenimine and related compounds. J. Am. Chem. Soc. 1953, 75, 2959;
-
(1953)
J. Am. Chem. Soc
, vol.75
, pp. 2959
-
-
Kissman, H.M.1
Tarbell, D.S.2
Williams3
-
28
-
-
2642668350
-
Synthesis of organic thiocyanates II: Synthesis of thiocyanate derivatives of phenols and naphthols
-
(c) Kaji, A. Synthesis of organic thiocyanates II: Synthesis of thiocyanate derivatives of phenols and naphthols. Nippon Kagaku Zasshi. 1961, 82, 382;
-
(1961)
Nippon Kagaku Zasshi
, vol.82
, pp. 382
-
-
Kaji, A.1
-
29
-
-
0142227938
-
Efficient conversion of substituted aryl thioureas to 2- aminobenzothiazoles using benzyltrimethylammonium tribromide
-
(d) Jordan, A. D.; Luo, C.; Reitz, A. B. Efficient conversion of substituted aryl thioureas to 2- aminobenzothiazoles using benzyltrimethylammonium tribromide. J. Org. Chem. 2003, 68, 8693.
-
(2003)
J. Org. Chem
, vol.68
, pp. 8693
-
-
Jordan, A.D.1
Luo, C.2
Reitz, A.B.3
|